DermaRite recalls PeriGuard Ointment (5g, 3.5oz, 7oz) due to contamination at shared manufacturing facility. Products with NDC 61924-205-05, 61924-205-04, or 61924-205-07 may be contaminated. Consumers should check product labels for affected lots.
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
DermaRite is recalling PeriGuard Ointment products that were made at a facility where contamination occurred. This could lead to skin exposure to harmful substances if the ointment is used without proper cleaning.
The ointment was manufactured at a facility that previously had contamination issues. This means the product could contain harmful substances that might cause skin irritation or infection if applied without proper cleaning.
People who own or use PeriGuard Ointment products with the listed NDC numbers (5g, 3.5oz, 7oz) are affected. Those with sensitive skin or using the ointment for medical purposes may be at higher risk.
Check the product label for the NDC numbers 61924-205-05 (5g), 61924-205-04 (3.5oz), or 61924-205-07 (7oz). Products with an expiration date of 08/2027 or earlier are affected.
Look for the NDC numbers 61924-205-05, 61924-205-04, or 61924-205-07 on the ointment tube.
The recall states there is a risk of contamination at the manufacturing facility, so it is not safe to use without checking the NDC numbers and following the recall instructions.
The recall does not specify a remedy, so you should check the product label for the NDC numbers and contact DermaRite if you have concerns.
Check the product label for the NDC numbers 61924-205-05 (5g), 61924-205-04 (3.5oz), or 61924-205-07 (7oz). Products with an expiration date of 08/2027 or earlier are affected.
We’ve drafted a message you can send DermaRite to request your refund or repair — edit it as you like.
Subject: Recall D-0173-2026 — DermaRite DermaRite Hello, I own a DermaRite that is covered by recall D-0173-2026 from DermaRite. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
